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Anticancer Efficacy of Photodynamic Therapy with Lung Cancer-Targeted Nanoparticles
Published on: December 1, 2016
Tumor Microenvironment-Responsive Nanomaterials as Targeted Delivery Carriers for Photodynamic Anticancer Therapy
Houhe Liu1, Jiwen Yao1, Huanhuan Guo1
1Key Laboratory of Molecular Target and Clinical Pharmacology, State Key Laboratory of Respiratory Disease, School of Pharmaceutical Science & Fifth Affiliated Hospital, Guangzhou Medical University, Guangzhou, China.
Abstract:
Photodynamic therapy (PDT), as an alternative approach to treat tumors through reactive oxygen species (ROS) produced by the activated photosensitizers (PS) upon light irradiation, has attracted wide attention in recent years due to its low invasive and highly efficient features. However, the low hydrophilicity and poor targeting of PS limits the clinical application of PDT. Stimuli-responsive nanomaterials represent a major class of remarkable functional nanocarriers for drug delivery. In particular, tumor microenvironment-responsive nanomaterials (TMRNs) can respond to the special pathological microenvironment in tumor tissues to release the loaded drugs, that allows them to control the release of PS within tumor tissues. Recent studies have demonstrated that TMRNs can achieve the targeted release of PS at tumor sites, increase the concentration of PS in tumor tissues, and reduce side effects of PDT. Hence, in the present paper, we review TMRNs, mainly including pH-, redox-, enzymes-, and hypoxia-responsive smart nanomaterials, and focus on the application of these smart nanomaterials as targeted delivery carriers of PS in photodynamic anticancer therapy, to further boost the development of PDT in tumor therapy.
Insights
Tumor microenvironment-responsive nanomaterials (TMRNs) enhance photodynamic therapy (PDT) by improving photosensitizer delivery to tumors. This targeted approach increases treatment efficacy and reduces side effects for better anticancer outcomes.
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Oncology
Background:
- Photodynamic therapy (PDT) uses photosensitizers (PS) and light to generate reactive oxygen species (ROS) for tumor treatment.
- Limitations of current PDT include poor photosensitizer hydrophilicity and targeting, hindering clinical application.
- Stimuli-responsive nanomaterials offer advanced drug delivery capabilities.
Purpose of the Study:
- To review tumor microenvironment-responsive nanomaterials (TMRNs) for targeted delivery of photosensitizers in photodynamic therapy.
- To explore the application of TMRNs in enhancing anticancer photodynamic therapy.
- To highlight the potential of TMRNs in overcoming current PDT limitations.
Main Methods:
- Review of recent studies on TMRNs, including pH-, redox-, enzyme-, and hypoxia-responsive nanomaterials.
- Focus on the use of these TMRNs as carriers for photosensitizers in anticancer PDT.
- Analysis of how TMRNs achieve targeted release and improve PS concentration at tumor sites.
Main Results:
- TMRNs demonstrate the ability to achieve targeted release of photosensitizers specifically within tumor tissues.
- These nanomaterials effectively increase photosensitizer concentration in tumors, leading to enhanced therapeutic effects.
- Targeted delivery by TMRNs significantly reduces the systemic side effects associated with conventional PDT.
Conclusions:
- TMRNs represent a promising strategy to improve the efficacy and safety of photodynamic therapy for cancer treatment.
- The development of stimuli-responsive nanomaterials is crucial for advancing targeted drug delivery in oncology.
- Further research into TMRNs will accelerate the clinical translation and broader application of photodynamic anticancer therapy.
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